“…4 In a recent retrospective review of methotrexate use in clinical practice, 50% of patients reported an adverse event while on therapy, with 32% of those being classified as "significant." 11 Day et al 12 proposed a classification system for ADRs secondary to low-dose methotrexate, dividing the ADRs into four distinct categories based on relation to dosing: type A-dose dependent, type B-idiosyncratic, type C-cumulative dose, and type D-delayed events after drug discontinuation. Our patient had multiple toxicities of pancytopenia, oral ulcerations, and cutaneous lesions in the setting of multiple risk factors including drug-drug interactions, acute renal failure, relative folate deficiency, and medication dosing errors.…”